Literature DB >> 24380058

Active Microscope Stabilization in Three Dimensions Using Image Correlation.

Ryan McGorty1, Daichi Kamiyama1, Bo Huang1.   

Abstract

BACKGROUND: Super-resolution microscopy techniques are often extremely susceptible to sample drift due to their high spatial resolution and the long time needed for data acquisition. While several techniques for stabilizing against drift exist, many require complicated additional hardware or intrusive sample preparations. We introduce a method that requires no additional sample preparation, is simple to implement and simultaneously corrects for x, y and z drift.
RESULTS: We use bright-field images of the specimen itself to calculate drift in all three dimensions: x, y and z. Bright-field images are acquired on an inexpensive CCD. By correlating each acquired bright-field image with an in-focus and two out-of-focus reference images we determine and actively correct for drift at rates of a few Hertz. This method can maintain stability to within 10 nm for x and y and 20 nm for z over several minutes.
CONCLUSION: Our active drift stabilization system is capable of simultaneously compensating x, y and z drift through an image-based correlation method that requires no special sample treatment or extensive microscope modifications. While other techniques may provide better stability, especially for higher frequency drift, our method is easy to implement and widely applicable in terms of both sample type and microscopy technique.

Entities:  

Keywords:  image correlation; stage stabilization; super-resolution microscopy

Year:  2013        PMID: 24380058      PMCID: PMC3874277          DOI: 10.1186/2192-2853-2-3

Source DB:  PubMed          Journal:  Opt Nanoscopy


  22 in total

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2.  Interferometric fluorescent super-resolution microscopy resolves 3D cellular ultrastructure.

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3.  Microscopy and its focal switch.

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4.  Live-cell photoactivated localization microscopy of nanoscale adhesion dynamics.

Authors:  Hari Shroff; Catherine G Galbraith; James A Galbraith; Eric Betzig
Journal:  Nat Methods       Date:  2008-04-13       Impact factor: 28.547

5.  Three-dimensional sub-100 nm resolution fluorescence microscopy of thick samples.

Authors:  Manuel F Juette; Travis J Gould; Mark D Lessard; Michael J Mlodzianoski; Bhupendra S Nagpure; Brian T Bennett; Samuel T Hess; Joerg Bewersdorf
Journal:  Nat Methods       Date:  2008-05-11       Impact factor: 28.547

6.  Sample drift correction in 3D fluorescence photoactivation localization microscopy.

Authors:  Michael J Mlodzianoski; John M Schreiner; Steven P Callahan; Katarina Smolková; Andrea Dlasková; Jitka Santorová; Petr Ježek; Joerg Bewersdorf
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7.  Breaking the diffraction barrier: super-resolution imaging of cells.

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8.  2,2'-thiodiethanol: a new water soluble mounting medium for high resolution optical microscopy.

Authors:  Thorsten Staudt; Marion C Lang; Rebecca Medda; Johann Engelhardt; Stefan W Hell
Journal:  Microsc Res Tech       Date:  2007-01       Impact factor: 2.769

9.  Endogenous activation patterns of Cdc42 GTPase within Drosophila embryos.

Authors:  Daichi Kamiyama; Akira Chiba
Journal:  Science       Date:  2009-06-05       Impact factor: 47.728

10.  Whole-cell 3D STORM reveals interactions between cellular structures with nanometer-scale resolution.

Authors:  Bo Huang; Sara A Jones; Boerries Brandenburg; Xiaowei Zhuang
Journal:  Nat Methods       Date:  2008-11-23       Impact factor: 28.547

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  24 in total

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2.  A Simple Marker-Assisted 3D Nanometer Drift Correction Method for Superresolution Microscopy.

Authors:  Hongqiang Ma; Jianquan Xu; Jingyi Jin; Yi Huang; Yang Liu
Journal:  Biophys J       Date:  2017-05-23       Impact factor: 4.033

3.  Localization events-based sample drift correction for localization microscopy with redundant cross-correlation algorithm.

Authors:  Yina Wang; Joerg Schnitzbauer; Zhe Hu; Xueming Li; Yifan Cheng; Zhen-Li Huang; Bo Huang
Journal:  Opt Express       Date:  2014-06-30       Impact factor: 3.894

4.  Specification of Dendritogenesis Site in Drosophila aCC Motoneuron by Membrane Enrichment of Pak1 through Dscam1.

Authors:  Daichi Kamiyama; Ryan McGorty; Rie Kamiyama; Michael D Kim; Akira Chiba; Bo Huang
Journal:  Dev Cell       Date:  2015-10-12       Impact factor: 12.270

5.  Axial plane single-molecule super-resolution microscopy of whole cells.

Authors:  Sha An; Karl Ferdinand Ziegler; Peiyi Zhang; Yu Wang; Tim Kwok; Fan Xu; Cheng Bi; Sandro Matosevic; Peng Yin; Tongcang Li; Fang Huang
Journal:  Biomed Opt Express       Date:  2019-12-23       Impact factor: 3.732

6.  Sample drift estimation method based on speckle patterns formed by backscattered laser light.

Authors:  Shih-Ya Chen; Rainer Heintzmann; Christoph Cremer
Journal:  Biomed Opt Express       Date:  2019-11-25       Impact factor: 3.732

Review 7.  Real-Time Feedback-Driven Single-Particle Tracking: A Survey and Perspective.

Authors:  Bertus van Heerden; Nicholas A Vickers; Tjaart P J Krüger; Sean B Andersson
Journal:  Small       Date:  2022-06-27       Impact factor: 15.153

8.  Single-molecule localization microscopy.

Authors:  Mickaël Lelek; Melina T Gyparaki; Gerti Beliu; Florian Schueder; Juliette Griffié; Suliana Manley; Ralf Jungmann; Markus Sauer; Melike Lakadamyali; Christophe Zimmer
Journal:  Nat Rev Methods Primers       Date:  2021-06-03

9.  Three-Dimensional Single-Molecule Localization Microscopy in Whole-Cell and Tissue Specimens.

Authors:  Sheng Liu; Hyun Huh; Sang-Hyuk Lee; Fang Huang
Journal:  Annu Rev Biomed Eng       Date:  2020-04-03       Impact factor: 9.590

10.  Imaging of In Vitro and In Vivo Neurons in Drosophila Using Stochastic Optical Reconstruction Microscopy.

Authors:  Melissa Ana Inal; Kathy Clara Bui; Abhijit Marar; Shaoheng Li; Peter Kner; Daichi Kamiyama
Journal:  Curr Protoc       Date:  2021-07
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